Status: current, Primitive. Date: 31-Jan 2013. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2923300016 | Hereditary dysplasia of blood vessel (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 2923303019 | Hereditary dysplasia of blood vessel | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary dysplasia of blood vessel | Is a | Vascular disorder | true | Inferred relationship | Some | ||
| Hereditary dysplasia of blood vessel | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| Hereditary dysplasia of blood vessel | Finding site | Blood vessel structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Osler haemorrhagic telangiectasia syndrome | Is a | True | Hereditary dysplasia of blood vessel | Inferred relationship | Some | |
| Klippel-Trenaunay-Weber syndrome | Is a | False | Hereditary dysplasia of blood vessel | Inferred relationship | Some | |
| Idiopathic arterial calcification of infancy | Is a | True | Hereditary dysplasia of blood vessel | Inferred relationship | Some | |
| Arterial tortuosity syndrome | Is a | True | Hereditary dysplasia of blood vessel | Inferred relationship | Some | |
| Grange syndrome | Is a | True | Hereditary dysplasia of blood vessel | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR